Creative Commons Attribution 4.0 International CC-BY-4.0 https://creativecommons.org/licenses/by/4.0/legalcode 164832 Orphanet classification of rare allergic disease 98050 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=98050 Rare allergic disease Category 658 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=658 Non-histaminic angioedema Clinical group 91378 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=91378 Hereditary angioedema Clinical group 528623 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=528623 Hereditary angioedema with C1Inh deficiency Disease 100050 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100050 Hereditary angioedema type 1 Etiological subtype 100051 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100051 Hereditary angioedema type 2 Etiological subtype 528647 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=528647 Hereditary angioedema with normal C1Inh Disease 100054 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100054 F12-related hereditary angioedema with normal C1Inh Clinical subtype 537072 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=537072 PLG-related hereditary angioedema with normal C1Inh Clinical subtype 599418 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=599418 Hereditary angioedema with normal C1Inh not related to F12 or PLG variant Clinical subtype 91385 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=91385 Acquired angioedema Clinical group 528663 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=528663 Acquired angioedema with C1Inh deficiency Disease 100055 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100055 Acquired angioedema type 2 Clinical subtype 100056 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100056 Acquired angioedema type 1 Clinical subtype 100057 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=100057 Renin-angiotensin-aldosterone system-blocker-induced angioedema Disease 79384 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=79384 Rare urticaria Category 2483 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2483 Melkersson-Rosenthal syndrome Malformation syndrome 64745 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=64745 Pruritic urticarial papules and plaques of pregnancy Disease 493342 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=493342 Vibratory urticaria Disease 98052 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=98052 Rare allergic respiratory disease Category 1164 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1164 Allergic bronchopulmonary aspergillosis Disease 2902 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2902 Idiopathic chronic eosinophilic pneumonia Disease 31740 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=31740 Hypersensitivity pneumonitis Disease 686462 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=686462 Non-fibrotic hypersensitivity pneumonitis Clinical subtype 686465 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=686465 Fibrotic hypersensitivity pneumonitis Clinical subtype 369992 http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=369992 Severe dermatitis-multiple allergies-metabolic wasting syndrome Disease